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For Clinical Researchers

Make the next handoff clearer.

  • Study Information, Patient Questions and Site Coordination
Discuss Your Site Workflow
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For Research Sites and Study Teams

Build the conversation around your published study.

Patients and clinicians may find your study while exploring their options. Fanoni invites research teams to discuss how public study information, patient questions and administrative handoffs could fit your site’s workflow.

Start with a defined collaboration. Your team retains screening, informed consent, enrollment and all study-visit decisions.

A defined research site handoff. Illustrative workflow: Clinical referrals require a separately approved workflow.

Clear study information. Clear responsibilities. A practical next step.

Discuss Site Collaboration
01

Published Study Details

Use the registration record, relevant locations and an appropriate site contact.
02

An Agreed Site Handoff

Define who receives inquiries and how patients are directed to your team.

Information, Communication and Coordination

A workflow your site can review.

Help People Understand Your Study

Discuss how published study details, registration numbers, recruiting locations and contact routes should inform patient questions. Explore source-linked information in Fanoni Care; trial listings must be checked with your team for current site availability.

Explore Public Study Information
Read the study. Check the source.. Illustrative workflow: A listing does not confirm suitability or eligibility.
A defined research site handoff. Illustrative workflow: Clinical referrals require a separately approved workflow.

Define Inquiry and Referral Handoffs

Agree the information needed for a general inquiry, the contact route and the responsibilities at each step. Any clinical referral workflow needs a separately approved channel and patient permission. This website does not receive clinical referrals or patient records.

Discuss Research Site Handoffs

Plan Administrative Follow-Up

Ask about support around calls, appointment communication and unanswered administrative questions. Confirm which steps Fanoni can support and which remain with your site. Your team manages screening, consent, enrollment and study visits.

Read About Research Site Coordination
Keep the practical steps together. Illustrative workflow: Every appointment needs provider confirmation.

Begin with one defined workflow.

Tell us about your site, the published study and the handoff you want to discuss. Agree service availability, responsibilities, contact permissions and any fees before coordination begins.

The proposed workflow is not an active referral-management platform, automated screening service or EHR/CTMS integration. No referral or enrollment volume is guaranteed.

Discuss Site Collaboration

Review Study Details

1

Define the Handoff

2

Agree Responsibilities

3

Confirm Follow-Up

4

Questions Before Your Next Step

Investigators, research coordinators and other study-site representatives can make a general professional inquiry. Include public study information and the workflow you want to discuss, without patient records or identifiable case details.

A general inquiry does not establish a referral program or guarantee qualified patients. Any future collaboration must define available services, consent, an approved information channel and handoff responsibilities. Your team makes eligibility and enrollment decisions.

No. Public research information helps people prepare questions. Your research team is responsible for protocol screening, informed consent, enrollment and study visits. We do not claim automated pre-screening accuracy or faster enrollment outcomes.

No. This website has no patient-record intake, EHR connection or CTMS integration. Use the form for general organizational questions. Any later clinical-data workflow needs separate agreement, permissions and an approved channel.

Discuss which administrative support is available and how it fits your site. Agree responsibilities, contact permissions and any fees before work starts. Appointments and study visits need your team’s confirmation.

No. It is a professional inquiry for the Fanoni team to review. Submitting this form does not book a call, create a platform account or establish a partnership.

Does Fanoni provide eligible participants to a research site?

Public study information can help people prepare an inquiry. A search result is not a screened referral. Any recruitment collaboration needs an agreed process; the study team assesses eligibility and manages enrollment.

Sources and Further Reading

These sources provide background. They do not endorse Fanoni or confirm access to a provider or study.

Speak With Fanoni

Tell us what your team needs.

A defined research site handoff. Illustrative workflow: Clinical referrals require a separately approved workflow.

Start with a general professional inquiry. We can discuss available support, responsibilities, permissions and any fees before work begins.

Explore Trial Information

Professional Inquiry

Your inquiry is saved in Fanoni’s private website inbox for the team to review. Keep your request general and do not include patient or medical details.

Keep this general. Do not include patient names, health records or other patient-identifying details. Maximum 1,000 characters.